US4397889A - Process for producing refractory powder - Google Patents

Process for producing refractory powder Download PDF

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US4397889A
US4397889A US06/365,685 US36568582A US4397889A US 4397889 A US4397889 A US 4397889A US 36568582 A US36568582 A US 36568582A US 4397889 A US4397889 A US 4397889A
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wax
particles
metal
binder
milling
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US06/365,685
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Mary Lou Benjamin
Robert J. Dobbs
Mary E. Shaffer
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Osram Sylvania Inc
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GTE Products Corp
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Assigned to GTE PRODUCTS CORPORATION reassignment GTE PRODUCTS CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: DOBBS, ROBERT JOHN, BENJAMIN, MARY LOU, SHAFFER, MARY E.
Priority to US06/365,685 priority Critical patent/US4397889A/en
Application filed by GTE Products Corp filed Critical GTE Products Corp
Priority to AT83102891T priority patent/ATE20201T1/en
Priority to DE8383102891T priority patent/DE3363892D1/en
Priority to EP83102891A priority patent/EP0091013B1/en
Priority to US06/520,094 priority patent/US4456484A/en
Priority to US06/520,095 priority patent/US4478888A/en
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F9/00Making metallic powder or suspensions thereof
    • B22F9/02Making metallic powder or suspensions thereof using physical processes
    • B22F9/04Making metallic powder or suspensions thereof using physical processes starting from solid material, e.g. by crushing, grinding or milling
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F1/00Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
    • B22F1/10Metallic powder containing lubricating or binding agents; Metallic powder containing organic material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F1/00Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
    • B22F1/10Metallic powder containing lubricating or binding agents; Metallic powder containing organic material
    • B22F1/108Mixtures obtained by warm mixing
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C1/00Making non-ferrous alloys
    • C22C1/04Making non-ferrous alloys by powder metallurgy
    • C22C1/05Mixtures of metal powder with non-metallic powder
    • C22C1/051Making hard metals based on borides, carbides, nitrides, oxides or silicides; Preparation of the powder mixture used as the starting material therefor
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F2998/00Supplementary information concerning processes or compositions relating to powder metallurgy

Definitions

  • Copending U.S. patent application Ser. No. 304,759 relates to a process wherein an aqueous mixture containing a dispersed phase of wax is attritor milled with metal carbide and metal binder particles to coat the particles with wax and produce a slurry which is spray dried to produce a powder.
  • the present invention relates to refractory powders, and particularly to refractory metal carbide grade powders of the type containing particles of refractory metal carbide, a binder metal and an organic binder.
  • Grade powders are pressed and sintered to form cemented carbide articles such as drill tools, cutting bits and wear parts.
  • Grade powders comprise a mixture of fine powders of metal carbides and a binder metal.
  • a wax binder may be included in the grade powder to promote the flowability of the grade powder into die cavities, to aid in pressing by a lubricating action, and to impart sufficient green strength to permit handling after pressing.
  • the wax binder Prior to sintering, the wax binder is typically removed during the step known as "dewaxing" by heating in a furnace at a temperature of from about ambient to 500° C. in a protective atmosphere or vacuum.
  • Paraffin type waxes which are insoluble in water are typically incorporated into grade powders by use of an organic solvent which dissolves the paraffin wax so that good dispersion of the wax in the powder is assured.
  • the organic fluid is removed by several drying methods to give a wax containing grade powder. Due to the flammability of organic solvents, if spray drying is used, a closed cycle spray drying system is required which utilizes an oxygen free atmosphere such as nitrogen. Generally, this system is characterized by a high initial cost as compared to a water system which can be an open system.
  • water is the milling liquid and a water soluble binder is utilized.
  • the water system is clearly desirable from a safety standpoint as compared to the organic system.
  • the water system is undesirably limited to the types of waxes that can be used since the waxes must be compatible with the system to adequately disperse the wax in the powder for achieving desired powder properties.
  • a process for producing a refractory powder containing an organic binder comprising heating particles of a refractory material to a temperature above the melting point and below the decomposition point of said organic binder to form a heated powder of refractory material, mixing said organic binder with said heated powder to form a blended mixture, milling said blended mixture with a liquid milling medium to produce a slurry, said organic binder being substantially insoluble in said liquid milling medium, and removing substantially all of said milling medium by evaporating below said decomposition temperature and forming a refractory powder comprising refractory particles having an adherent coating of organic binder.
  • a process for producing a powder mixture of metal carbide particles, metal binder particles and wax suitable for making a cemented metal carbide comprising heating a mixture of refractory metal carbide particles to a temperature above the melting point of said wax to form a heated powder, mixing said wax with said heated powder to form a blended mixture, milling said blended mixture including metal binder particles with a liquid milling medium to produce a slurry, said wax being substantially insoluble in said liquid milling medium, and drying said slurry to remove said milling medium and form a powder mixture comprising metal carbide particles and metal binder particles and said wax.
  • Grade powders which may be prepared by the process of the present invention are intimate mixtures of refractory metal carbide powders plus a metallic cementing phase or matrix called a metal binder.
  • the grade powders include an organic binder which also serves as a pressing lubricant.
  • a typical grade powder is a mixture of tungsten carbide, cobalt, and paraffin wax.
  • the carbide powder may consist of other carbides or mixtures thereof and are generally the refractory carbides which include carbides of the metals from the Groups IV, V and VI of the Periodic Table that have a melting point above about 1895° C. Cobalt is the most common matrix for tungsten carbide.
  • Nickel, iron, and molybdenum, either singularly or in combination, particularly in combination with cobalt are typically used when refractory metal carbides other than tungsten carbide are used.
  • the matrix phase for titanium carbide is typically either nickel or a nickel-molybdenum alloy.
  • the matrix metal is selected from the iron group of metals and alloys of the iron group of metals.
  • the amount of binder metal or matrix metal may be from about 2 to about 90 percent by weight of the total weight of refractory carbide and matrix metal. From about 5 to about 20 percent is more typical.
  • the average particle size of the refractory metal carbide is generally from slightly less than one micron to about 25 microns.
  • the most common tungsten carbide generally is between 1 to 2 microns.
  • Grain inhibitors and other additives may typically be employed in the grade powder mix. Materials commonly used are molybdenum carbide, vanadium carbide and chromium carbide.
  • the refractory metal particles may be conveniently blended with the metal binder particles to form a blended power mixture. It is also contemplated that additions of binder metal or metal carbide particles may be performed during subsequent mixing operations.
  • Grade powders may be processed by any suitable method known in the art to produce a hard body that is particularly desirable for use as the working surfaces of tools.
  • sintered metal carbide bodies are prepared by pressing the grade power in hard steel or carbide lined steel molds at pressures usually ranging from 5 to 30 tons per square inch depending on the size and shape of the compact. Sintering is then performed usually at temperatures ranging from 1350° to 1500° C. for times of from about 30 to 60 minutes. Sintering is generally performed in a protected or non-oxidizing atmosphere.
  • waxes utilized in the process of the present invention is insoluble in water.
  • Typical water-insoluble waxes are low-melting mixtures or compounds of high molecular weight which are solid at room temperature and generally similar in composition to fats and oils.
  • the waxes are thermoplastic and possess the properties of water repellency, smooth texture, and nontoxicity.
  • the major types of waxes include animal wax such as bees wax, spermaceti, lanolin, and shellac wax.
  • the vegetable waxes include carnauba, candelilla, and others.
  • Mineral waxes include earth waxes such as ceresin and petroleum waxes such as paraffin.
  • Various synthetic waxes include ethylenic polymers, polyol ether-esters, chlorinated naphthalenes and various hydrocarbon waxes.
  • water-insoluble waxes petroleum waxes such as paraffin waxes are preferred.
  • the water-insoluble waxes are typically soluble in organic solvents such as acetone.
  • Typical organic solvent-insoluble waxes include polyglycol, polyethylene glycol, hydroxyethylcellulose, tapioca starch, and carboxymethylcellulose. Some of the organic-insoluble waxes may be soluble in water.
  • metal carbide particles which may include metal binder particles are heated to a temperature above the melting point of the wax and intimately or thoroughly mixed to form a substantially uniform blend of heated carbide powder and wax.
  • the temperature is at least about 20 degrees centigrade and more preferably about 30 degrees centigrade above the melting point of the wax.
  • the temperature should be below the decomposition temperatures of the wax. Generally longer mixing times tend to give a better dispersion of the wax in the powder.
  • the metal carbide particles and wax should be sufficiently mixed so that the particles are at least partially coated with or imbedded in the wax. If metal binder particles are present with metal carbide particles, the mixing should be carried out in a non-oxidizing environment, i.e.
  • the amount of wax typically used should be sufficient to impart green strength to a pressed compact. Increased amounts of wax up to a certain level tend to increase the green strength of a compact.
  • the amount of wax varies according to the type of desired grade powder. The amount of wax employed is typically from about 0.5 to about 5 percent by weight based on the total weight of the final grade powder.
  • the uniformly blended mixture of wax and metal carbide is preferably cooled.
  • the cooling promotes adherence of wax to particles. Tumbling during cooling aids in obtaining smaller clumps of mix. Cooling also reduces tendency of metal binder oxidation.
  • Milling the resulting blended metal carbide containing wax and metal binder powder is an important feature of the present invention. If metal binder is not present during the heating and mixing of wax and metal carbide particles, metal binder particles are added either prior to or during milling to produce a milled mixture of metal carbide, metal binder and wax.
  • the milling of relatively coarse fraction of refractory material is often desirable to reduce the powder to a particle size suitable for sintering.
  • the refractory material is a metal carbide
  • compactability of alloy powders is improved by milling with a metal binder.
  • the milling mixture is milled with a liquid milling medium to produce a slurry.
  • the liquid milling medium is selected so that the wax is insoluble therein.
  • the hereinbefore waxes insoluble in water may be used when water is a milling fluid. When other waxes hereinbefore mentioned are used, an incompatible or insoluble fluid is utilized.
  • the milling is attritor milling.
  • Attritor milling aids in rapidly dispersing the metal binder throughout the powder.
  • the time required to properly disperse the metal binder particles or reduce the particle size during attritor milling is dependant on the particular attritor mill used, the type of powders used, the speed of the mill and various other factors. Generally it has been found that times as short as one hour are sufficient to properly disperse the particles and obtain a desirable size reduction.
  • the slurry is discharged from the mill. This may require additional milling fluid to thin the slurry and rinse the mill. During discharge, the slurry may be passed through a 100 mesh screen to permit the removal of any contamination than may have been introduced from the milling balls. Milling fluid may be decanted from the screened slurry to obtain the desired solids concentration for spray drying. Generally, this ranges from 70-90% by weight. It is desirable to avoid using excess milling fluid during milling so that the drying step may be carried out without prior decanting or filtering.
  • Spray drying may be carried out using commercially available spray drying equipment.
  • the inlet and outlet air temperatures should be maintained below about 370° C. and 190° C., respectively, to prevent substantial oxidation or decarburization of the slurry constituents.
  • the spray drying is carried out under conditions to produce an agglomerated powder mixture consisting essentially of aglomerated particles of metal carbide, metal binder and wax. Typically the size range of the agglomerated particles is from about 20 to about 150 microns.
  • the slurry is generally heated to about 50° C. and agitated.
  • a suitable spray dryer is a Protco-Schwartz spray dryer with two-fluid-top nozzle atomization.
  • typical drying parameters may be an air pressure of 20 psi, drying temperature of 200°-230° C. and an outlet temperature of 100°-130° C.
  • the spray drying is preferably performed in absent air. Spray drying temperatures are dependent on the volatility of the solvent.
  • the spray dried agglomerates may be classified by screening to obtain a desired fraction.
  • the milling fluid may be conveniently evaporatively removed at a temperature below the decomposition temperature of the organic binder.
  • the milled refractory powder and binder may be tumbled during evaporative drying to prevent formation of agglomerates.
  • the drying should be carried out to such an extent that substantially all the milling fluid is removed from the powder.
  • the powder consists essentially of refractory particles, organic binder and intentional additives.
  • tungsten carbide powder is placed in a Ross double-planetary mixer equipped with a heating/cooling jacket.
  • the tungsten carbide powder is pre-heated to a temperature of 165° C.
  • About 3.6 kilograms of synthetic amide wax is added.
  • the wax which is insoluble in water is obtained from Kindt Collins Co. and has a melting point of about 135° C.
  • the mixing is continued for about 5 minutes after addition of the wax while the temperature is maintained at about 160° C.
  • the wax-metal carbide mixture is mixed additionally while the mixer is changed to a cooling mode and the powder mixture is cooled to room temperature.
  • About 25 liters of deionized water is placed in an attritor mill and the mill is rotated at slow speed.
  • the waxed metal carbide powder and 10.8 kilograms of cobalt metal powder are slowly added and dispersed in the milling solution.
  • the mill is then rotated at high speed, about 100 r.p.m. for about 1/2 to 3 hours.
  • the slurry is removed from the mill and transferred to a holding tank where it is agitated prior to spraying.
  • the spray drying results in the formation of agglomerated particles of metal carbide, metal binder and wax which are suitable for pressing into compacts and sintering.
  • tungsten carbide powder is placed in a heater mixer and heated to 90° C. The temperature is maintained while about 6 grams of Carbowax 8000, a polyethylene glycol which is water soluble with a melting point about 65° C., is added. The mixing is continued for another 5 minutes while the 90° C. temperature is maintained. The mixer is changed to a cooling mode to cool the tungsten carbide-wax mixture to room temperature. Mixing is continued during cooling to prevent the formation of large agglomerates. About 180 milliliters of heptane is placed in an attritor mill. The carbowax is insoluble in the heptane.
  • the tungsten carbide-wax mixture and about 18 grams of cobalt powder are slowly added to the mill.
  • the powders are permitted to disperse in the milling medium for a short period of time.
  • the mill is then rotated at high speed, about 200 r.p.m. for about 2 hours.
  • the slurry is removed and placed in a pan which is dried over a steam table while spatulating.
  • the powder produced in a non-agglomerated powder of tungsten carbide, metal binder particles and wax.

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  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
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Abstract

In a process for producing a refractory metal carbide grade powder, a metal carbide powder is heated above melting point of a wax prior to forming a blended mixture of metal carbide and wax which is subsequently milled with a metal binder in liquid milling medium incompatible with the wax and the mixture is dried to form a powder.

Description

CROSS REFERENCE TO RELATED APPLICATIONS
Copending U.S. patent application Ser. No. 304,759 relates to a process wherein an aqueous mixture containing a dispersed phase of wax is attritor milled with metal carbide and metal binder particles to coat the particles with wax and produce a slurry which is spray dried to produce a powder.
The present invention relates to refractory powders, and particularly to refractory metal carbide grade powders of the type containing particles of refractory metal carbide, a binder metal and an organic binder.
BACKGROUND OF THE INVENTION
Grade powders are pressed and sintered to form cemented carbide articles such as drill tools, cutting bits and wear parts. Grade powders comprise a mixture of fine powders of metal carbides and a binder metal. A wax binder may be included in the grade powder to promote the flowability of the grade powder into die cavities, to aid in pressing by a lubricating action, and to impart sufficient green strength to permit handling after pressing.
Prior to sintering, the wax binder is typically removed during the step known as "dewaxing" by heating in a furnace at a temperature of from about ambient to 500° C. in a protective atmosphere or vacuum.
As set forth in U.S. Pat. No. 4,070,184 to Scheithauer et al. a process is described wherein water is used as a milling fluid and a water soluble, long chain polyvinyl alcohol is added to the milled slurry of metal carbide and binder metal after milling but prior to spray drying. According to this process, the wax-like binder is water soluble or compatible with water to ensure adequate distribution of the wax in the grade powder.
Paraffin type waxes which are insoluble in water are typically incorporated into grade powders by use of an organic solvent which dissolves the paraffin wax so that good dispersion of the wax in the powder is assured. The organic fluid is removed by several drying methods to give a wax containing grade powder. Due to the flammability of organic solvents, if spray drying is used, a closed cycle spray drying system is required which utilizes an oxygen free atmosphere such as nitrogen. Generally, this system is characterized by a high initial cost as compared to a water system which can be an open system.
In the water system, water is the milling liquid and a water soluble binder is utilized. The water system is clearly desirable from a safety standpoint as compared to the organic system. However, the water system is undesirably limited to the types of waxes that can be used since the waxes must be compatible with the system to adequately disperse the wax in the powder for achieving desired powder properties.
It is desirable to develop systems for waxing grade powders which permit more flexibility in the utilization of waxes.
SUMMARY OF INVENTION
In accordance with the present invention, there is provided a process for producing a refractory powder containing an organic binder comprising heating particles of a refractory material to a temperature above the melting point and below the decomposition point of said organic binder to form a heated powder of refractory material, mixing said organic binder with said heated powder to form a blended mixture, milling said blended mixture with a liquid milling medium to produce a slurry, said organic binder being substantially insoluble in said liquid milling medium, and removing substantially all of said milling medium by evaporating below said decomposition temperature and forming a refractory powder comprising refractory particles having an adherent coating of organic binder.
In accordance with a more particular aspect of the present invention, there is provided a process for producing a powder mixture of metal carbide particles, metal binder particles and wax suitable for making a cemented metal carbide comprising heating a mixture of refractory metal carbide particles to a temperature above the melting point of said wax to form a heated powder, mixing said wax with said heated powder to form a blended mixture, milling said blended mixture including metal binder particles with a liquid milling medium to produce a slurry, said wax being substantially insoluble in said liquid milling medium, and drying said slurry to remove said milling medium and form a powder mixture comprising metal carbide particles and metal binder particles and said wax.
DETAILED DESCRIPTION
Grade powders which may be prepared by the process of the present invention are intimate mixtures of refractory metal carbide powders plus a metallic cementing phase or matrix called a metal binder. Generally the grade powders include an organic binder which also serves as a pressing lubricant. A typical grade powder is a mixture of tungsten carbide, cobalt, and paraffin wax. The carbide powder may consist of other carbides or mixtures thereof and are generally the refractory carbides which include carbides of the metals from the Groups IV, V and VI of the Periodic Table that have a melting point above about 1895° C. Cobalt is the most common matrix for tungsten carbide. Nickel, iron, and molybdenum, either singularly or in combination, particularly in combination with cobalt are typically used when refractory metal carbides other than tungsten carbide are used. For example, the matrix phase for titanium carbide is typically either nickel or a nickel-molybdenum alloy. As used herein, the matrix metal is selected from the iron group of metals and alloys of the iron group of metals.
The amount of binder metal or matrix metal may be from about 2 to about 90 percent by weight of the total weight of refractory carbide and matrix metal. From about 5 to about 20 percent is more typical.
The average particle size of the refractory metal carbide is generally from slightly less than one micron to about 25 microns. The most common tungsten carbide generally is between 1 to 2 microns. Grain inhibitors and other additives may typically be employed in the grade powder mix. Materials commonly used are molybdenum carbide, vanadium carbide and chromium carbide. The refractory metal particles may be conveniently blended with the metal binder particles to form a blended power mixture. It is also contemplated that additions of binder metal or metal carbide particles may be performed during subsequent mixing operations.
Grade powders may be processed by any suitable method known in the art to produce a hard body that is particularly desirable for use as the working surfaces of tools. Typically sintered metal carbide bodies are prepared by pressing the grade power in hard steel or carbide lined steel molds at pressures usually ranging from 5 to 30 tons per square inch depending on the size and shape of the compact. Sintering is then performed usually at temperatures ranging from 1350° to 1500° C. for times of from about 30 to 60 minutes. Sintering is generally performed in a protected or non-oxidizing atmosphere.
One type of waxes utilized in the process of the present invention is insoluble in water. Typical water-insoluble waxes are low-melting mixtures or compounds of high molecular weight which are solid at room temperature and generally similar in composition to fats and oils. The waxes are thermoplastic and possess the properties of water repellency, smooth texture, and nontoxicity. The major types of waxes include animal wax such as bees wax, spermaceti, lanolin, and shellac wax. The vegetable waxes include carnauba, candelilla, and others. Mineral waxes include earth waxes such as ceresin and petroleum waxes such as paraffin. Various synthetic waxes include ethylenic polymers, polyol ether-esters, chlorinated naphthalenes and various hydrocarbon waxes. Of the water-insoluble waxes petroleum waxes such as paraffin waxes are preferred. The water-insoluble waxes are typically soluble in organic solvents such as acetone.
Another type of waxes utilized in the process of the present invention is insoluble in organic solvents. Typical organic solvent-insoluble waxes include polyglycol, polyethylene glycol, hydroxyethylcellulose, tapioca starch, and carboxymethylcellulose. Some of the organic-insoluble waxes may be soluble in water.
In accordance with the present invention, metal carbide particles which may include metal binder particles are heated to a temperature above the melting point of the wax and intimately or thoroughly mixed to form a substantially uniform blend of heated carbide powder and wax. Preferably the temperature is at least about 20 degrees centigrade and more preferably about 30 degrees centigrade above the melting point of the wax. The temperature should be below the decomposition temperatures of the wax. Generally longer mixing times tend to give a better dispersion of the wax in the powder. The metal carbide particles and wax should be sufficiently mixed so that the particles are at least partially coated with or imbedded in the wax. If metal binder particles are present with metal carbide particles, the mixing should be carried out in a non-oxidizing environment, i.e. inert atmosphere or vacuum to prevent the oxidation of the metal binder. The amount of wax typically used should be sufficient to impart green strength to a pressed compact. Increased amounts of wax up to a certain level tend to increase the green strength of a compact. The amount of wax varies according to the type of desired grade powder. The amount of wax employed is typically from about 0.5 to about 5 percent by weight based on the total weight of the final grade powder.
Next the uniformly blended mixture of wax and metal carbide is preferably cooled. The cooling promotes adherence of wax to particles. Tumbling during cooling aids in obtaining smaller clumps of mix. Cooling also reduces tendency of metal binder oxidation.
Milling the resulting blended metal carbide containing wax and metal binder powder is an important feature of the present invention. If metal binder is not present during the heating and mixing of wax and metal carbide particles, metal binder particles are added either prior to or during milling to produce a milled mixture of metal carbide, metal binder and wax. The milling of relatively coarse fraction of refractory material is often desirable to reduce the powder to a particle size suitable for sintering. When the refractory material is a metal carbide, compactability of alloy powders is improved by milling with a metal binder. The milling mixture is milled with a liquid milling medium to produce a slurry. The liquid milling medium is selected so that the wax is insoluble therein. The hereinbefore waxes insoluble in water may be used when water is a milling fluid. When other waxes hereinbefore mentioned are used, an incompatible or insoluble fluid is utilized.
Preferably the milling is attritor milling. Attritor milling aids in rapidly dispersing the metal binder throughout the powder. The time required to properly disperse the metal binder particles or reduce the particle size during attritor milling is dependant on the particular attritor mill used, the type of powders used, the speed of the mill and various other factors. Generally it has been found that times as short as one hour are sufficient to properly disperse the particles and obtain a desirable size reduction.
After the appropriate milling time, the slurry is discharged from the mill. This may require additional milling fluid to thin the slurry and rinse the mill. During discharge, the slurry may be passed through a 100 mesh screen to permit the removal of any contamination than may have been introduced from the milling balls. Milling fluid may be decanted from the screened slurry to obtain the desired solids concentration for spray drying. Generally, this ranges from 70-90% by weight. It is desirable to avoid using excess milling fluid during milling so that the drying step may be carried out without prior decanting or filtering.
Spray drying may be carried out using commercially available spray drying equipment. The inlet and outlet air temperatures should be maintained below about 370° C. and 190° C., respectively, to prevent substantial oxidation or decarburization of the slurry constituents. The spray drying is carried out under conditions to produce an agglomerated powder mixture consisting essentially of aglomerated particles of metal carbide, metal binder and wax. Typically the size range of the agglomerated particles is from about 20 to about 150 microns. During spray drying, the slurry is generally heated to about 50° C. and agitated. A suitable spray dryer is a Protco-Schwartz spray dryer with two-fluid-top nozzle atomization. When water is the milling fluid, typical drying parameters may be an air pressure of 20 psi, drying temperature of 200°-230° C. and an outlet temperature of 100°-130° C. When organic solvents are used as the milling fluid, the spray drying is preferably performed in absent air. Spray drying temperatures are dependent on the volatility of the solvent. The spray dried agglomerates may be classified by screening to obtain a desired fraction.
Although spray drying is the preferred method of drying, it is contemplated that other drying methods which produce an agglomerate or a non-agglomerate may be utilized. The milling fluid may be conveniently evaporatively removed at a temperature below the decomposition temperature of the organic binder. When it is desirable to produce a non-agglomerated powder, the milled refractory powder and binder may be tumbled during evaporative drying to prevent formation of agglomerates. The drying should be carried out to such an extent that substantially all the milling fluid is removed from the powder. The powder consists essentially of refractory particles, organic binder and intentional additives.
To more fully illustrate the invention, the following example is presented. All parts, proportions, and percentages are by weight unless otherwise indicated.
EXAMPLE 1
About 169 kilograms of tungsten carbide powder is placed in a Ross double-planetary mixer equipped with a heating/cooling jacket. The tungsten carbide powder is pre-heated to a temperature of 165° C. About 3.6 kilograms of synthetic amide wax is added. The wax which is insoluble in water is obtained from Kindt Collins Co. and has a melting point of about 135° C. The mixing is continued for about 5 minutes after addition of the wax while the temperature is maintained at about 160° C. The wax-metal carbide mixture is mixed additionally while the mixer is changed to a cooling mode and the powder mixture is cooled to room temperature. About 25 liters of deionized water is placed in an attritor mill and the mill is rotated at slow speed. The waxed metal carbide powder and 10.8 kilograms of cobalt metal powder are slowly added and dispersed in the milling solution. The mill is then rotated at high speed, about 100 r.p.m. for about 1/2 to 3 hours. The slurry is removed from the mill and transferred to a holding tank where it is agitated prior to spraying. The spray drying results in the formation of agglomerated particles of metal carbide, metal binder and wax which are suitable for pressing into compacts and sintering.
EXAMPLE 2
About 282 grams of tungsten carbide powder is placed in a heater mixer and heated to 90° C. The temperature is maintained while about 6 grams of Carbowax 8000, a polyethylene glycol which is water soluble with a melting point about 65° C., is added. The mixing is continued for another 5 minutes while the 90° C. temperature is maintained. The mixer is changed to a cooling mode to cool the tungsten carbide-wax mixture to room temperature. Mixing is continued during cooling to prevent the formation of large agglomerates. About 180 milliliters of heptane is placed in an attritor mill. The carbowax is insoluble in the heptane. While the mill is rapidly rotated, the tungsten carbide-wax mixture and about 18 grams of cobalt powder are slowly added to the mill. The powders are permitted to disperse in the milling medium for a short period of time. The mill is then rotated at high speed, about 200 r.p.m. for about 2 hours. The slurry is removed and placed in a pan which is dried over a steam table while spatulating. The powder produced in a non-agglomerated powder of tungsten carbide, metal binder particles and wax.

Claims (13)

We claim:
1. A process for producing a refractory powder containing an organic binder comprising heating particles of a refractory material to a temperature above the melting point and below the decomposition temperature of said organic binder to form a heated powder of refractory material, said organic binder consisting essentially of a wax, mixing said organic binder with said heated powder to form a blended mixture, milling said blended mixture with a liquid milling medium to produce a slurry, said organic binder being substantially insoluble in said liquid milling medium, and removing substantially all of said milling medium by evaporation below the decomposition temperature of said organic binder to form a refractory powder having an adherent coating of said organic binder.
2. A process for producing a powder mixture of metal carbide particles, metal binder particles and wax suitable for making a cemented metal carbide comprising forming a mixture of metal carbide particles and wax at a temperature above the melting point of said wax, said metal carbide particles and wax being sufficiently mixed to form a blended mixture of wax and metal carbide particles, milling said blended mixture including metal binder particles with a liquid milling medium to substantially uniformly disperse said metal binder particles and to produce a slurry, said metal binder particles being added prior to or during milling, said wax being substantialy insoluble in said liquid milling medium, drying said slurry to remove said milling medium and produce a powder comprising particles of metal carbide, metal binder and wax.
3. A process to claim 2 wherein said mixture of metal carbide particles and wax includes metal binder particles, and said mixture is sufficiently mixed in a non-oxidizing environment to form a blended mixture of wax, metal binder particles and metal carbide particles.
4. A process according to claim 2 wherein said metal binder particles are added to said blended mixture of wax and metal carbide particles after mixing.
5. A process according to claim 4 wherein said drying comprises spray drying to produce an agglomerated powder.
6. A process according to claim 5 wherein said wax is water insoluble and said milling medium comprises water.
7. A process according to claim 6 wherein said wax comprises a parafin wax.
8. A process according to claim 5 wherein said milling medium comprises an organic solvent and said wax is insoluble in said organic solvent.
9. A progress according to claim 1 wherein said temperature of heating is at least about 20 degrees centigrade above the melting point of said organic binder.
10. A process according to claim 9 wherein said temperature of heating is at least about 30 degrees centigrade above the melting point of said organic binder.
11. A process according to claim 10 wherein said blended mixture is cooled prior to milling.
12. A process according to claim 11 wherein said milling comprises attritor milling.
13. A process according to claim 12 wherein evaporation comprises spray drying.
US06/365,685 1982-04-05 1982-04-05 Process for producing refractory powder Expired - Lifetime US4397889A (en)

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AT83102891T ATE20201T1 (en) 1982-04-05 1983-03-23 PROCESS FOR PRODUCTION OF A CARBIDE POWDER.
EP83102891A EP0091013B1 (en) 1982-04-05 1983-03-23 Process for producing refractory powder
DE8383102891T DE3363892D1 (en) 1982-04-05 1983-03-23 Process for producing refractory powder
US06/520,094 US4456484A (en) 1982-04-05 1983-08-04 Process for producing refractory powder
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Cited By (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4716019A (en) * 1987-06-04 1987-12-29 Gte Products Corporation Process for producing composite agglomerates of molybdenum and molybdenum carbide
US4724121A (en) * 1985-04-25 1988-02-09 Aluminum Company Of America Powder treatment process
US4902471A (en) * 1989-09-11 1990-02-20 Gte Products Corporation Method for producing metal carbide grade powders
US4906294A (en) * 1987-04-21 1990-03-06 Fried. Krupp Gesellschaft Mit Beschrankter Haftung Cutting tool produced by sintering a blank formed by a pressing tool
US4963183A (en) * 1989-03-03 1990-10-16 Gte Valenite Corporation Corrosion resistant cemented carbide
WO1997028918A1 (en) * 1996-02-12 1997-08-14 Credo Tool Company Method of making a carbide cutting insert
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WO1998018973A1 (en) * 1996-10-25 1998-05-07 Sandvik Ab (Publ) Method of making cemented carbide by powder injection molding
US5922978A (en) * 1998-03-27 1999-07-13 Omg Americas, Inc. Method of preparing pressable powders of a transition metal carbide, iron group metal or mixtures thereof
WO2002079531A2 (en) * 2001-03-29 2002-10-10 Plansee Tizit Aktiengesellschaft Method for producing a hard metal projection
WO2002079532A2 (en) * 2001-03-29 2002-10-10 Plansee Tizit Aktiengesellschaft Method for producing hard metal granulated material
US20040156736A1 (en) * 2002-10-26 2004-08-12 Vlad Ocher Homogeneous shaped charge liner and fabrication method
US6814903B1 (en) 2000-03-10 2004-11-09 Parker Gerard E Low-firing temperature method for producing AL2O3 bodies having enhanced chemical resistance
US20060091579A1 (en) * 2004-11-04 2006-05-04 Zschimmer & Schwarz Gmbh & Co. Kg Chemische Fabriken Liquid and its use for the preparation of hard metals
US20060101945A1 (en) * 2003-02-10 2006-05-18 Ceratizit Austria Gesellschaft M.B.H. Method for producing a hard metal stock
US20060272451A1 (en) * 2005-05-17 2006-12-07 Sandvik Intellectual Property Ab Method of making agglomerated cemented carbide powder mixtures
US20070131567A1 (en) * 2005-12-09 2007-06-14 Park Chan S High temperature and pressure sensor
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US20140113140A1 (en) * 2011-05-30 2014-04-24 Jingmen Gem New Material Co., Ltd Coated cobalt powder and preparation method thereof
EP2857124A1 (en) 2013-10-03 2015-04-08 Kennametal Inc. Aqueous slurry for making a powder of hard material
EP2860274A2 (en) 2013-10-04 2015-04-15 Kennametal India Limited Hard material and method of making the same from an aqueous hard material milling slurry
JP2017527687A (en) * 2014-06-12 2017-09-21 マシネンファブリーク グスタフ アイリッヒ ゲーエムベーハー ウント コー. カーゲーMaschinenfabrik Gustav Eirich Gmbh & Co.Kg New method for making cemented carbide or cermet body
CN115365491A (en) * 2022-08-29 2022-11-22 浙江旗创新材料科技有限公司 Efficient powder premixing process

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3051566A (en) * 1959-01-20 1962-08-28 Gen Electric Process for producing high density refractory bodies
US3962491A (en) * 1972-10-11 1976-06-08 Aisin Chemical Company, Limited Process for producing resin-coated sand particles for use in shell moles
US4070184A (en) * 1976-09-24 1978-01-24 Gte Sylvania Incorporated Process for producing refractory carbide grade powder
US4284431A (en) * 1977-08-05 1981-08-18 Kabushiki Kaisha Komatsu Seisakusho Method for the production of sintered powder ferrous metal preform
JPS6010842A (en) * 1983-06-29 1985-01-21 Fujitsu Ltd Pulse counter control system

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB303751A (en) * 1928-01-07 1930-02-13 British Thomson Houston Co Ltd Improvements in and relating to hard metal compositions
GB683037A (en) * 1949-06-29 1952-11-19 British Thomson Houston Co Ltd Improvements in and relating to methods and apparatus for introducing lubricant into powdered materials
US4230462A (en) * 1978-12-08 1980-10-28 Ford Motor Company Method of improving tool life of TiC base tools
JPS5738896A (en) * 1980-08-15 1982-03-03 Sumitomo Chem Co Ltd Composite binder composition for powder molding

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3051566A (en) * 1959-01-20 1962-08-28 Gen Electric Process for producing high density refractory bodies
US3962491A (en) * 1972-10-11 1976-06-08 Aisin Chemical Company, Limited Process for producing resin-coated sand particles for use in shell moles
US4070184A (en) * 1976-09-24 1978-01-24 Gte Sylvania Incorporated Process for producing refractory carbide grade powder
US4284431A (en) * 1977-08-05 1981-08-18 Kabushiki Kaisha Komatsu Seisakusho Method for the production of sintered powder ferrous metal preform
JPS6010842A (en) * 1983-06-29 1985-01-21 Fujitsu Ltd Pulse counter control system

Cited By (43)

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US4724121A (en) * 1985-04-25 1988-02-09 Aluminum Company Of America Powder treatment process
US4906294A (en) * 1987-04-21 1990-03-06 Fried. Krupp Gesellschaft Mit Beschrankter Haftung Cutting tool produced by sintering a blank formed by a pressing tool
US4716019A (en) * 1987-06-04 1987-12-29 Gte Products Corporation Process for producing composite agglomerates of molybdenum and molybdenum carbide
US4963183A (en) * 1989-03-03 1990-10-16 Gte Valenite Corporation Corrosion resistant cemented carbide
US4902471A (en) * 1989-09-11 1990-02-20 Gte Products Corporation Method for producing metal carbide grade powders
US5809848A (en) * 1996-02-12 1998-09-22 Credo Tool Company Method of making a carbide cutting insert
WO1997028918A1 (en) * 1996-02-12 1997-08-14 Credo Tool Company Method of making a carbide cutting insert
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EP0800882A2 (en) * 1996-04-09 1997-10-15 Basf Aktiengesellschaft Process for preparing granulate and articles from hard metal or cermet material
EP0800882A3 (en) * 1996-04-09 1999-02-03 Basf Aktiengesellschaft Process for preparing granulate and articles from hard metal or cermet material
WO1998018973A1 (en) * 1996-10-25 1998-05-07 Sandvik Ab (Publ) Method of making cemented carbide by powder injection molding
US5922978A (en) * 1998-03-27 1999-07-13 Omg Americas, Inc. Method of preparing pressable powders of a transition metal carbide, iron group metal or mixtures thereof
WO1999065840A2 (en) * 1998-03-27 1999-12-23 Omg Americas, Inc. Method of preparing pressable powders of a transition metal carbide, iron group metal or mixtures thereof
WO1999065840A3 (en) * 1998-03-27 2000-01-27 Omg Americas Method of preparing pressable powders of a transition metal carbide, iron group metal or mixtures thereof
US6814903B1 (en) 2000-03-10 2004-11-09 Parker Gerard E Low-firing temperature method for producing AL2O3 bodies having enhanced chemical resistance
US6733562B2 (en) 2001-03-29 2004-05-11 Ceratizit Austria Gmbh Method of producing hard metal grade powder
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US20030061906A1 (en) * 2001-03-29 2003-04-03 Gerhard Knunz Method for producing hard metal granulate
US20030075012A1 (en) * 2001-03-29 2003-04-24 Gerhard Knunz Method of producing hard metal grade powder
WO2002079532A2 (en) * 2001-03-29 2002-10-10 Plansee Tizit Aktiengesellschaft Method for producing hard metal granulated material
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US6852274B2 (en) 2001-03-29 2005-02-08 Ceratizit Austria Gesellschaft M.B.H. Method for producing hard metal granulate
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US20060101945A1 (en) * 2003-02-10 2006-05-18 Ceratizit Austria Gesellschaft M.B.H. Method for producing a hard metal stock
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CN115365491B (en) * 2022-08-29 2024-05-17 浙江旗创新材料科技有限公司 Efficient powder premixing process

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ATE20201T1 (en) 1986-06-15

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